A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066379



Internal ID19155598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60735891..60807941hg38UCSC Ensembl
Innerchr18:58403124..58475174hg19UCSC Ensembl
Innerchr18:56554104..56626154hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3872051
hg1972051
hg1872051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565617, nssv3565618
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066379
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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